Luminescence lifetime imaging of oxygen, pH, and carbon dioxide distribution using optical sensors

被引:169
作者
Liebsch, G
Klimant, I [1 ]
Frank, B
Holst, G
Wolfbeis, OS
机构
[1] Univ Regensburg, Inst Analyt Chemo Biosensors, D-93040 Regensburg, Germany
[2] Max Planck Inst Marine Microbiol, D-28359 Bremen, Germany
关键词
optical sensor films; time-resolved imaging system; microsecond decay time sensors;
D O I
10.1366/0003702001949726
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
We present a modular system for time-resolved two-dimensional luminescence lifetime imaging of planar optical chemical sensors. It is based on a fast, gateable charge-coupled device (CCD) camera without image intensifier and a pulsable light-emitting diode (LED) array as a light source. Software was developed for data acquisition with a maximum of parameter variability and for background suppression. This approach allows the operation of the system even under daylight. Optical sensors showing analyte-specific changes of their luminescence decay time were tested and used for sensing pO(2), pCO(2), pH, and temperature. The luminophores employed are either platinum(II)-porphyrins or ruthenium(II)-polypyridyl completes, contained in polymer films, and can be efficiently excited by blue LEDs. The decay times of the sensor films vary from 70 mu s far the Pt(II)-porphyrins to several 100 ns for the Ru(II) complexes. In a typical application, 7 mm-diameter spots of the respective optical sensor films were placed at the bottom of the wells of microtiterplates. Thus, every well represents a separate calibration chamber with an integrated sensor element. Both luminescence intensity-based and time-resolved images of the sensor spots were evaluated and compared. The combination of optical sensor technology with time-resolved imaging allows a determination of the distribution of chemical or physical parameters in heterogeneous systems and is therefore a powerful tool for screening and mapping applications.
引用
收藏
页码:548 / 559
页数:12
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